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4-((1,3,6,7-Tetramethoxyxanthone-4-yl)-sulfonyl)-(2R,6S)-2,6-dimethyl-morpholine ID: ALA1096715
PubChem CID: 46887524
Max Phase: Preclinical
Molecular Formula: C23H27NO9S
Molecular Weight: 493.53
Molecule Type: Small molecule
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: COc1cc2oc3c(S(=O)(=O)N4C[C@@H](C)O[C@@H](C)C4)c(OC)cc(OC)c3c(=O)c2cc1OC
Standard InChI: InChI=1S/C23H27NO9S/c1-12-10-24(11-13(2)32-12)34(26,27)23-19(31-6)9-18(30-5)20-21(25)14-7-16(28-3)17(29-4)8-15(14)33-22(20)23/h7-9,12-13H,10-11H2,1-6H3/t12-,13+
Standard InChI Key: GLWCNHCKGJYPPI-BETUJISGSA-N
Molfile:
RDKit 2D
34 37 0 0 0 0 0 0 0 0999 V2000
5.7445 -13.3651 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.3190 -12.6558 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4887 -12.6728 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.0918 -13.3951 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.5694 -13.3512 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
5.7182 -11.9338 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.5430 -11.9184 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.2670 -13.4116 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.8402 -12.7056 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.3439 -14.0868 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.5164 -14.0998 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1161 -14.8189 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.7711 -14.7930 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.2912 -14.8307 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.3663 -15.5168 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.5412 -15.5258 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1382 -16.2438 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.5593 -16.9532 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.3875 -16.9401 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.7868 -16.2216 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1567 -17.6733 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.3318 -17.6848 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8115 -17.6479 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.4105 -18.3689 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.9939 -14.0586 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
6.9750 -12.6333 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.1500 -12.6333 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.5933 -14.7806 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.0142 -15.4859 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.8395 -15.4763 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.2421 -14.7551 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.8195 -14.0436 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.0670 -14.7441 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6110 -16.2057 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16 17 1 0
4 8 1 0
17 18 2 0
3 4 2 0
18 19 1 0
8 9 1 0
19 20 2 0
20 15 1 0
10 11 2 0
18 21 1 0
4 11 1 0
21 22 1 0
1 2 2 0
19 23 1 0
1 5 1 0
23 24 1 0
10 1 1 0
5 25 1 0
10 13 1 0
5 26 2 0
11 12 1 0
5 27 2 0
25 28 1 0
12 16 1 0
15 13 1 0
2 6 1 0
12 14 2 0
2 3 1 0
25 32 1 0
28 29 1 0
29 30 1 0
30 31 1 0
31 32 1 0
6 7 1 0
31 33 1 1
15 16 2 0
29 34 1 1
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 493.53Molecular Weight (Monoisotopic): 493.1407AlogP: 2.78#Rotatable Bonds: 6Polar Surface Area: 113.74Molecular Species: NEUTRALHBA: 9HBD: ┄#RO5 Violations: ┄HBA (Lipinski): 10HBD (Lipinski): ┄#RO5 Violations (Lipinski): ┄CX Acidic pKa: ┄CX Basic pKa: ┄CX LogP: 2.00CX LogD: 2.00Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.48Np Likeness Score: -0.06
References 1. Hu H, Liao H, Zhang J, Wu W, Yan J, Yan Y, Zhao Q, Zou Y, Chai X, Yu S, Wu Q.. (2010) First identification of xanthone sulfonamides as potent acyl-CoA:cholesterol acyltransferase (ACAT) inhibitors., 20 (10): [PMID:20403694 ] [10.1016/j.bmcl.2010.03.101 ] 2. Pokhrel, Laxman and 5 more authors. 2012-10-25 Inhibition of Acyl-CoA: cholesterol acyltransferase (ACAT), overexpression of cholesterol transporter gene, and protection of amyloid β (Aβ) oligomers-induced neuronal cell death by tricyclic pyrone molecules. [PMID:23025824 ] 3. Ting, Pauline C PC and 10 more authors. 2013-02-15 Lead optimization of a pyridine-carboxamide series as DGAT-1 inhibitors. [PMID:23317570 ] 4. Eguchi, Keisuke K and 10 more authors. 2013-07-01 Manzamine A, a marine-derived alkaloid, inhibits accumulation of cholesterol ester in macrophages and suppresses hyperlipidemia and atherosclerosis in vivo. [PMID:23665143 ]